FDA Device recall Z-0231-2015
Etest¿ Ceftaroline (CPT32) WWB100
- FDA Device
- Class III
- terminated
- Published 2014-11-26
On 2014-11-26 the FDA classified a Class III recall of Etest¿ Ceftaroline (CPT32) WWB100 by Biomerieux, citing the products have a wrong expiration date on their labeling, 5 years instead of 2 years.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0231-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-10-16 |
| Published | 2014-11-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomerieux |
| Distribution | US |
Product
Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
Reason
The products have a wrong expiration date on their labeling, 5 years instead of 2 years.
Identifiers
| code_info | Ref #537508, Lot #1003160510, Right Expiry date: 27-APR-2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0231-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.